| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:50623887-50624079 | Common:1; Rare:76 | ||||
| chr10:50991106-50991381 | Common:4; Rare:79 | ||||
| chr10:51074364-51074566 | Common:1; Rare:45; Clinvar (benign):2 | ||||
| chr10:51699563-51699829 | Common:3; Rare:72 | ||||
| chr10:52314073-52314283 | Common:1; Rare:53 | ||||
| chr10:56361223-56361518 | Common:7; Rare:107 | ||||
| chr10:62049209-62049482 | Common:1; Rare:61 | ||||
| chr10:63269156-63269388 | Common:2; Rare:50 | ||||
| chr10:63465972-63466149 | Common:1; Rare:82 | ||||
| chr10:68331911-68332115 | Common:1; Rare:88 | ||||
| chr10:68332890-68332958 | Common:1; Rare:20 | ||||
| chr10:68407252-68407440 | Common:4; Rare:59 | ||||
| chr10:68721006-68721248 | Common:1; Rare:77 | ||||
| chr10:69416909-69417054 | Common:3; Rare:44 | ||||
| chr10:70403996-70404155 | Rare:59 |